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理解少数族裔社区的痴呆症:作为 IDEAL 项目一部分接受采访的主要利益相关者的观点。

Understanding dementia in minority ethnic communities: The perspectives of key stakeholders interviewed as part of the IDEAL programme.

机构信息

Department of Health Sciences, College of Health, Medicine and Life Sciences, Brunel University London, London, UK.

University of Exeter Medical School, University of Exeter, Exeter, UK.

出版信息

Dementia (London). 2024 Oct;23(7):1172-1182. doi: 10.1177/14713012241272817. Epub 2024 Aug 17.

Abstract

Future populations of older adults in the UK, those aged 65+, will demonstrate increased diversity in terms of their ethnic identity resultant from the ageing of the post-war migrants from India, Pakistan, Bangladesh, and the Caribbean. As a consequence, there will be an increase in the numbers of older adults from these communities living with age-related chronic diseases such as dementia. In response to these demographic changes, we need to develop a research, policy and practice agenda that is inclusive and provides evidence for the development of culturally diverse and effective models of service delivery. This requires engagement with three key stakeholder groups: (a) people with dementia; (b) their carers; and (c) the wider community. As part of the IDEAL research programme on living well with dementia, we undertook semi-structured interviews with twelve community leaders, defined as known and trusted individuals active in their respective communities, and six community members (two people living with dementia and four carers). We explored their understandings, experiences, and views of about dementia. Our analysis identified two overarching themes. The migrant lifecourse highlighted issues of not belonging, discrimination and racism. This framed our second theme, the cultural context of dementia, which addressed dementia knowledge and attitudes, service provision and service access, and how being part of a minority ethnic community made a difference to these experiences. Our study highlights how lifecourse experiences of negative hostile social and policy environments and services can be profound and long-lasting and provide a prism through which accessing dementia care is experienced. Our findings argue for the inclusion of diverse views and lifecourse experiences within the context of developing a dementia strategy for research, policy and practice that is appropriate for a multicultural and heterogenous society.

摘要

未来英国的老年人口(65 岁以上)将在种族身份方面呈现出更多的多样性,这是由于战后来自印度、巴基斯坦、孟加拉国和加勒比地区的移民老龄化所导致的。因此,来自这些社区的患有与年龄相关的慢性疾病(如痴呆症)的老年人口数量将会增加。为了应对这些人口变化,我们需要制定一个研究、政策和实践议程,使其具有包容性,并为发展文化多样化和有效的服务提供证据。这需要与三个关键利益相关者群体进行接触:(a)痴呆症患者;(b)他们的照顾者;和(c)更广泛的社区。作为 IDEAL 痴呆症生活计划的一部分,我们对 12 名社区领袖进行了半结构化访谈,这些社区领袖被定义为在各自社区中活跃的知名和受信任的个人,以及 6 名社区成员(2 名患有痴呆症的人和 4 名照顾者)。我们探讨了他们对痴呆症的理解、经验和看法。我们的分析确定了两个总体主题。移民的生活历程突出了归属感缺失、歧视和种族主义问题。这构成了我们的第二个主题,即痴呆症的文化背景,它涉及痴呆症知识和态度、服务提供和服务获取,以及作为少数族裔社区的一员如何对这些经历产生影响。我们的研究强调了生活历程中负面敌对的社会和政策环境和服务经历是如何深刻而持久的,并提供了一个棱镜,通过这个棱镜来体验获得痴呆症护理的经历。我们的研究结果表明,在制定适合多元文化和异质社会的研究、政策和实践痴呆症战略时,应纳入多样化的观点和生活历程经验。

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